Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Tigecycline
Drug ID BADD_D02217
Description Tigecycline is a glycylcycline antibiotic developed and marketed by Wyeth under the brand name Tygacil. It was developed in response to the growing prevalence of antibiotic resistance in bacteria such as Staphylococcus aureus. It was granted fast-track approval by the U.S. Food and Drug Administration (FDA) on June 17, 2005.
Indications and Usage For the treatment of infections caused by susceptible strains of the designated microorganisms in the following conditions: Complicated skin and skin structure infections caused by Escherichia coli, Enterococcus faecalis (vancomycin-susceptible isolates only), Staphylococcus aureus (methicillin-susceptible and -resistant isolates), Streptococcus agalactiae, Streptococcus anginosus grp. (includes S. anginosus, S. intermedius, and S. constellatus), Streptococcus pyogenes and Bacteroides fragilis. Complicated intra-abdominal infections caused by Citrobacter freundii, Enterobacter cloacae, Escherichia coli, Klebsiella oxytoca, Klebsiella pneumoniae, Enterococcus faecalis (vancomycin-susceptible isolates only), Staphylococcus aureus (methicillin-susceptible isolates only), Streptococcus anginosus grp. (includes S. anginosus, S. intermedius, and S. constellatus), Bacteroides fragilis, Bacteroides thetaiotaomicron, Bacteroides uniformis, Bacteroides vulgatus, Clostridium perfringens, and Peptostreptococcus micros.
Marketing Status approved
ATC Code J01AA12
DrugBank ID DB00560
KEGG ID D01079
MeSH ID D000078304
PubChem ID 54686904
TTD Drug ID D0G4OD
NDC Product Code 67680-002; 63323-960; 70121-1647; 71288-019; 55150-228; 0781-3481; 0008-4990; 58623-0048; 63415-0134; 68225-013; 60505-6098; 60715-1001; 16729-364; 0008-4994; 70600-002; 44657-0055
UNII 70JE2N95KR
Synonyms Tigecycline | TBG-MINO | 9-(tert-Butylglycylamido)minocycline | Tygacil | GAR 936 | GAR-936 | GAR936
Chemical Information
Molecular Formula C29H39N5O8
CAS Registry Number 220620-09-7
SMILES CC(C)(C)NCC(=O)NC1=CC(=C2CC3CC4C(C(=O)C(=C(C4(C(=O)C3=C(C2=C1O)O)O)O)C(=O)N)N(C) C)N(C)C
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice.
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Abdominal distension07.01.04.001--
Abdominal pain07.01.05.002--
Abnormal faeces07.01.03.001---
Abscess11.01.08.001---
Acidosis14.01.03.002--
Activated partial thromboplastin time13.01.02.033---
Activated partial thromboplastin time prolonged13.01.02.001--
Acute hepatic failure09.01.03.0010.000073%-
Alanine aminotransferase increased13.03.04.005--
Amylase increased13.05.01.009--
Anaemia01.03.02.001--
Anaphylactic reaction10.01.07.001; 24.06.03.006--
Anaphylactic shock10.01.07.002; 24.06.02.004---
Anaphylactoid reaction10.01.07.003; 24.06.03.007---
Aspartate aminotransferase increased13.03.04.011--
Asthenia08.01.01.001---
Atrial fibrillation02.03.03.002--
Atrioventricular block first degree02.03.01.004--
Azotaemia20.01.01.001---
Back pain15.03.04.005--
Blood alkaline phosphatase13.04.02.010---
Blood creatine phosphokinase increased13.04.01.001--
Blood creatinine increased13.13.01.004--
Blood lactate dehydrogenase increased13.04.02.002--
Blood urea increased13.13.01.006---
Body temperature increased13.15.01.001---
Bradycardia02.03.02.0020.000097%-
Bronchiectasis22.03.02.0050.000049%-
Bronchospasm10.01.03.012; 22.03.01.0040.000049%
Cardiac arrest02.03.04.0010.000073%
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ADReCS-Target
Drug Name ADR Term Target
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